Needle placement manipulator with attachment for rf-coil

ABSTRACT

A needle placement manipulator includes, a needle holder configured to hold a needle, a guide system configured to position the needle holder to a predetermined direction with respect to a subject of needle placement, an attachment including an attaching portion to which the guide system is attached and a setting portion on which an RF-coil is set. A base surface of the setting portion is configured to be disposed on the subject.

BACKGROUND

1. Field

The disclosure of this application relates generally to medical devices, and in particular it relates to a needle placement manipulator and a needle placement manipulator with attachment for RF-coil.

2. Related Art

The use of imaging modalities, such as ultrasound, mammography, computed tomography (CT), Magnetic Resonance Imaging (MRI) and the like, to assist in identifying and treating abnormalities within the body of a patient, has gained increased acceptance in the medical field. The above-named and other imaging modalities generally provide good contrast between different soft tissues of the body. Thus, many of these techniques are being used to depict the boundaries of damaged tissue within healthy tissue for accurate identification and treatment. Advanced diagnostic procedures, however, require further validation and refinement in localization of damaged tissue. This further validation and advanced localization can be performed by needle biopsy procedures. To help define the boundaries of damaged tissue within healthy tissue with greater accuracy, needle guidance systems have been proposed.

A non-patent literature article entitled “MRI Guided Needle Insertion—Comparison of Four Techniques”, by Fisher et al., describes four techniques for needle placement: 1) image overlay that projects an MR image and virtual needle guide on the patient, 2) biplane laser with needle trajectory marked by intersecting transverse and oblique sagittal lasers, 3) handheld protractor with pre-angled guide sleeve, and 4) freehand insertion. Conventionally, all of these techniques have required removing the patient out the imaging modality for needle insertion.

In the medical environment, it is necessary to position a needle tip precisely inside tissue or a specific organ for accurate diagnosis or minimal invasive therapy. Biopsy, ablation, cryotherapy, aspiration and drug delivery are examples that require high precision needle placement. Prior to a percutaneous incision, a target area of interest (e.g., tumor, nodule, etc.) is confirmed by means of non-invasive imaging with MRI, ultrasound or other imaging modality. Once the target area of interest is positively determined, the clinician decides an entry point, inserting direction and depth to be reached by the needle based on experience. This process often requires a lengthy trial and error routine, which can be deleterious to the patient. Accordingly, in the last few decades there has been an increased interest in the development of needle guiding systems that can improve accuracy of needle positioning, minimize patient discomfort, and shorten time of operation.

In the realm of needle guiding systems having a handheld protractor with pre-angled guide sleeve, US Patent Application Publication 2011/0190787 disclosed by Hirdesh Sahni (herein “Sahni”) is an example. Sahni describes an “IMAGE GUIDED WHOLE BODY STEREOTACTIC NEEDLE PLACEMENT DEVICE with FALLING ARC”. In Sahni's system, the device may be compatible with both CT and MRI modalities, but the patient has to hold the breath while the needle is being passed into regions that move on respiration. The device can be placed on the skin or on near an exposed organ of a patient, but its function can be jeopardized by movement.

In the realm of modality-guided needle placement systems, US Patent Application Publication 2006/0229641 disclosed by Rajiv Gupta et al., (herein “Gupta”) is an example. Gupta describes a “GUIDANCE AND INSERTION SYSTEM”, in which the insertion angle of the needle is guided by two arc-shaped arms which are driven by motors respectively attached at the axis of each arm. The device can be configured for use with an imaging apparatus, such as CT scanner, to allow the device and tool to be operated while viewing the device positioned in relation to a target surgical site. The device can be placed on a patient's skin and fastened by belts. The device can passively compensate for patient's movement.

In MRI-guided percutaneous interventions, accurate needle placement is of great concern and of considerably more difficulty that in needle placement systems for other modalities, such as CT or ultrasound. Unlike other modalities, MRI makes use of the property of nuclear magnetic resonance (NMR) to image nuclei of atoms inside the body. To that end, during an MRI scan, a patient is disposed within a powerful magnet where a large magnetic field is used to align the magnetization of atomic nuclei in the patient's body, and a radio frequency (RF) pulse is applied to alter the linear magnetization of the atomic nuclei. This causes the atomic nuclei to absorb energy from tuned radiofrequency pulses, and emit radiofrequency signals as their excitation decays. These signals, which vary in intensity according to nuclear abundance and molecular chemical environment, are converted into sets of tomographic (selected planes) images by using field gradients in the magnetic field, which in turn permits 3-dimensional (3D) localization of the point sources of the signals (or damaged tissue). More specifically, the detected signals are used to construct 2D or 3D MRI images of the scanned area of the body.

In an MRI-guided needle placement system, therefore, it is preferred that the entire positioning system consists essentially of non-magnetic materials such that there is no danger of impairing the homogeneity of the magnetic field within an examination volume. In addition, in order to track spatial positioning of the needle with respect to the guiding system, it is necessary to provide a marking point, such as a MR measurable fiduciary mechanically rigidly connected to the guiding system. In this manner, the position of the manipulator itself can be determined via MR measurement. U.S. Pat. No. 6,185,445 to Knuttel discloses and example of such system.

Shortcomings of conventional technology include: 1. When applying the needle placement manipulator to MR-image guided intervention, the manipulator and an RF-coil must be placed without interference between with each other. The manipulator needs to be configured to fit with the RF-coil. The manipulator should be placed on top of RF-coils, and it should be removable so that a clinician's workspace for observations and interventions will not be limited, and so that the clinician can observe the patient through the opening of the RF-coil. The number of steps with which the RF-coil and the manipulator are positioned on the patient (the subject of the needle insertion) should be minimized to shorten the procedure, for the convenience of the patient and the clinician. The position and orientation of the needle with respect to the subject of needle placement should be precisely repeatable. The needle placement manipulator should be made of materials which do not interfere with the magnetic field of the MRI scanner.

SUMMARY

According to at least one embodiment of the present application, a needle placement manipulator includes, a needle holder configured to hold a needle, a guide system configured to position the needle holder to a predetermined direction with respect to a subject of needle placement, an attachment including an attaching portion to which the guide system is attached and a setting portion on which an RF-coil is set. A base surface of the setting portion is configured to be disposed on the subject.

Further features of the present invention will become apparent from the following description of exemplary embodiments with reference to the attached drawings.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1 illustrates a needle placement manipulator according to a first embodiment;

FIGS. 2A and 2B illustrates cross-sectional views of the needle placement manipulator according to the first embodiment. FIG. 2C illustrates an angular relationship between the rotational axes of rotary guides and a needle holder axis;

FIGS. 3A, 3B and 3C illustrate examples of needle insertion at a single crossing point with various angles of insertion;

FIGS. 4A and 4B illustrate a maximum angle of inclination 63 and optimal rotational space determined by the maximum angle of inclination 63;

FIGS. 5A and 5B are sectional views of a needle placement manipulator equipped with a motorized actuator, according to a second embodiment;

FIG. 6A illustrates a detailed sectional view of the left side of FIG. 5A. FIG. 6B illustrates a detailed sectional view of the left side of FIG. 5A using optical fibers;

FIG. 7A illustrates an example of a motorized needle manipulator including set screws for locking the rotational guides in a stopped position, according to a modification of the second embodiment. FIG. 7B illustrates an example of a motorized needle manipulator in which the base body includes a sliding portion to adjust a height of the crossing point, according to a further modification of the second embodiment;

FIG. 8A illustrates a perspective view of needle manipulator attached to an RF-coil, according to third embodiment; FIG. 8B illustrates a sectional cut along vertical plane H-H of the needle manipulator attached to an RF-coil;

FIG. 9A illustrates a sectional view of the needle manipulator cut along a vertical plane H-H, according to the third embodiment. FIG. 9B illustrates a detailed view of section A shown in FIG. 9A where a first attachment 30 engages with a second attachment 31 on an outer surface thereof. FIG. 9C illustrates a detailed view of section A shown in FIG. 9A where a first attachment 30 engages with a second attachment 31 on an inner surface thereof;

FIGS. 10A, 10B and 10C illustrates an exemplary procedure for attaching and detaching a needle manipulator to an RF-coil with attachments therefor;

FIG. 11 illustrates a perspective view of the assembled needle manipulator attached to the RF-coil with first and second attachments engaged to each other;

FIG. 12 illustrates a sectional view of a motorized needle manipulator attached to an RF-coil, in accordance with the fourth embodiment; and

FIG. 13 illustrates a block diagram of an automated image-guided needle positioning system which includes a needle manipulator.

DETAILED DESCRIPTION

In the following description, reference is made to the accompanying drawings which are illustrations of embodiments in which the disclosed invention may be practiced. It is to be understood, however, that those skilled in the art may develop other structural and functional modifications without departing from the novelty and scope of the instant disclosure.

In referring to the description, specific details are set forth in order to provide a thorough understanding of the examples disclosed. In other instances, well-known methods, procedures, components and circuits have not been described in detail as not to unnecessarily lengthen the present disclosure. Some embodiments of the present invention may be practiced on a computer system that includes, in general, one or a plurality of processors for processing information and instructions, random access (volatile) memory (RAM) for storing information and instructions, read-only (non-volatile) memory (ROM) for storing static information and instructions, a data storage device such as a magnetic or optical disk and disk drive for storing information and instructions, an optional user output device such as a display device (e.g., a monitor) for displaying information to the computer user, an optional user input device including alphanumeric and function keys (e.g., a keyboard) for communicating information and command selections to the processor, and an optional user input device such as a cursor control device (e.g., a mouse) for communicating user input information and command selections to the processor.

As will be appreciated by those skilled in the art, the present examples may be embodied as a system, method or computer program product. Accordingly, some examples may take the form of an entirely hardware embodiment, and entirely software embodiment (including firmware, resident software, micro-code, etc.) or an embodiment combining software and hardware aspects that may all generally be referred herein as a “circuit”, “module” or “system”. Further, some embodiments may take the form of a computer program product embodied in any tangible medium of expression having computer-usable program code stored therein. For example, some embodiments described below with reference to flowchart illustrations and/or block diagrams of methods, apparatus (systems) and computer program products can be implemented by computer program instructions. The computer program instructions may be stored in computer-readable media that can direct a computer or other programmable data processing apparatus to function in a particular manner, such that the instructions stored in the computer-readable media constitute an article of manufacture including instructions and processes which implement the function/act/step specified in the flowchart and/or block diagram.

It should be understood that if an element or part is referred herein as being “on”, “against”, “connected to”, or “coupled to” another element or part, then it can be directly on, against, connected or coupled to the other element or part, or intervening elements or parts may be present. In contrast, if an element is referred to as being “directly on”, “directly connected to”, or “directly coupled to” another element or part, then there are no intervening elements or parts present. When used, term “and/or”, includes any and all combinations of one or more of the associated listed items, if so provided.

Spatially relative terms, such as “under” “beneath”, “below”, “lower”, “above”, “upper”, “proximal”, “distal”, and the like, may be used herein for ease of description and/or illustration to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the various figures. It should be understood, however, that the spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if the device in the figures is turned over, elements described as “below” or “beneath” other elements or features would then be oriented “above” the other elements or features. Thus, a relative spatial term such as “below” can encompass both an orientation of above and below. The device may be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein are to be interpreted accordingly. Similarly, the relative spatial terms “proximal” and “distal” may also be interchangeable, where applicable.

The terms first, second, third, etc. may be used herein to describe various elements, components, regions, parts and/or sections. It should be understood that these elements, components, regions, parts and/or sections should not be limited by these terms. These terms have been used only to distinguish one element, component, region, part, or section from another region, part, or section. Thus, a first element, component, region, part, or section discussed below could be termed a second element, component, region, part, or section without departing from the teachings herein.

The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting. As used herein, the singular forms “a”, “an”, and “the”, are intended to include the plural forms as well, unless the context clearly indicates otherwise. It should be further understood that the terms “includes” and/or “including”, when used in the present specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof not explicitly stated.

In describing example embodiments illustrated in the drawings, specific terminology is employed for the sake of clarity. However, the disclosure of this patent specification is not intended to be limited to the specific terminology so selected and it is to be understood that each specific element includes all technical equivalents that operate in a similar manner.

Exemplary embodiments will be described below with reference to the several drawings, where like reference numerals refer to like parts.

First Embodiment

The first embodiment of the present invention is directed to a solution for the issues mentioned above. FIG. 1 is a perspective view of a needle placement manipulator 100 in accordance with the first embodiment. FIGS. 2A and 2B are sectional views of the needle placement manipulator at different operating positions.

As illustrated in FIG. 1, according to the first embodiment, a needle placement manipulator 100 includes two circular ring-shaped rotary guides (hereinafter referred simply to as “rotary guides”), which are arranged in a slanted orientation with respect to each other atop a base body 5. Specifically, a first rotary guide 1 and a second rotary guide 3 are arranged in a slanted orientation with respect to each other. The two rotary guides 1 and 3 are supported by a base body 5. The base body 5 is preferably a non-magnetic structure configured to be mounted on a patient's skin 8. As discussed in more detail below, the base body 5 and certain other elements can be manufactured of disposable and recyclable materials, such as plastics and/or composites thereof. The first rotary guide 1 is supported by the base body 5 and connects to a first rotation body 2. The second rotary guide 3 is supported by the first rotation body 2 and connects to a second rotation body 4. The second rotation body 4 is configured to support a needle holder 6. The needle holder 6 has a thru hole 6 b configured to guide a needle 7 therethrough. The needle holder 6 constrains the needle 7 to align to selected angle geometrically determined by rotation of the two rotary guides 1 and 3.

The first rotation body 2 in this embodiment consists of three pillars 2 a, 2 b and 2 c. But it is not limited to this structure. The first rotation body 2 can be formed of other structures, for example, one pillar or plurality of pillars, or a shell structure or a shell structure with holes. Many other shapes and structures may be readily available to a person having ordinary skill in the art. Notably, however, when the rotation body 2 consists of one or at most three pillars, as illustrated in FIG. 1, an ample opening for viewing an incision point is advantageously provided. Similarly, the second rotation body 4 consists of one or more pillars connecting the needle holder 7 to the second rotary guide 3.

Each of the rotary guides 1 and 3 respectively includes a set of rotational devices 13 and 23, and a fixing element 1 b and 3 b. Rotational devices promote easy rotation of the rotary guides to a desired position; and the fixing elements hold the rotary guides fixed in the desired position to prevent movement during a needle incision operation. In this embodiment, fixing elements 1 b and 3 b are set screws, and the rotational devices 13 and 23 are mechanical bearings. In preparation for an incision operation, a clinician or an automated actuator manipulates at least one the two rotary guides (the guides can operate independently from each other) to rotate the needle holder 6 to a predetermined angle. Once the desired position is reached, the rotary guides are fixed by tightening the fixing elements (screws) 1 b and 3 b, so that the needle holder 6 is directed to a desired angle to reach a target tissue 8 a under the patient's skin 8. In this embodiment, fixing means are set screws. Air-clutches also can be used as fixing means instead of screws. The air clutch is rotation-free when air-pressure is supplied from an air-supply source like a compressed gas cylinder or a medical air supply outlet in the surgical room; and when the air-supply is shut, the air-clutch holds the rotation of the rotary guides fixed.

Referring back to FIG. 1, markers 10 a, 10 b, 10 c, 10 d, 10 e, 10 f, 10 g and 10 h are MRI-visible fiducial markers which are arranged at predetermined locations on the base body 5, and first rotary guide 1, and the second rotary guide 3. During an MRI-guided intervention, images of these markers are acquired by MRI-scanner to obtain the spatial position and posture of each of these parts. Slits 5 a and 5 b provided within the base body 5 are slits for a belt to fasten the manipulator to patient's body.

In this embodiment in FIG. 1, the base body 5 is fixed to patient's body by fastening belts. But fastening is not limited to the belts only. The manipulator can be fastened to a patient's body by bolts passing through slits 5 a and 5 b to be fixed to bone of patients, or adhered to the patient by adhesive tapes, suction cups, and so on. It is also can be fixed to patient's bed or floor by a passive arm which can hold its joints by air clutch.

As illustrated in FIG. 2A, the first rotary guide 1 rotates around a fixed rotational axis 1 a. And the second rotary guide 3 rotates around a fixed rotational axis 3 a. The term “fixed rotational axis”, as used herein, means that the axis of rotation is fixed with respect to its corresponding rotating part. The needle holder 6 includes the thru-hole 6 b through which a needle holder axis 6 a passes longitudinally. The axis 1 a of first rotary guide 1, the axis 3 a of second rotary guide 3, and the axis 6 a of the needle holder 6 are arranged to always cross at a single crossing point 9 located at the center of gravity of the base body 5. As used herein, the term “center of gravity” refers to the point at which all the surrounding weight is equal. That is, it is the point at which an object is in balance.

In operation, the direction of the needle is determined by two angles of the rotary guides 1 and 3 without changing the crossing point 9. In FIG. 2A, the needle holder axis 6 a is substantially perpendicular to the base body 5, and thus also substantially perpendicular to the first rotary guide 1. It can be said therefore, that at a given first position the needle holder axis 6 a can be made substantially perpendicular to the first rotary guide 1. In this first position, the needle holder axis 6 a can be made to substantially coincide with the axis 1 a. From this given first position, the needle holder axis 6 a and consequentially the needle holder 6 can be moved to any position between the initial perpendicular position (FIG. 2A) and a maximum inclined position illustrated in FIG. 2B.

FIG. 2C illustrates the angular relationship between the rotational axis 1 a of the first rotary guide 1, the rotational axis 3 a of the second rotary guide 3 and the needle holder axis 6 a of the needle holder 6. As illustrated in FIG. 2C, all of the axis 1 a, 3 a and 6 a coincide and are fixed at the crossing point 9. Here, it should be understood that the rotational axis 1 a of the first rotary guide 1 and the rotational axis 3 a of the second rotary guide 3 are preferably fixed with respect to each other. However, the needle holder axis 6 a of the needle holder 6 is not fixed and can be moved around the axis 3 a and/or the axis 1 a.

In the position illustrated in FIGS. 2B and 2C, θ1 is the angle between the rotational axis 1 a of the first rotary guide 1 and the rotational axis 3 a of the second rotary guide 3; and θ2 is the angle between the rotational axis 3 a of the second rotary guide 3 and the needle holder axis 6 a of the needle holder 6, when the needle holder axis 6 a is at its maximum inclined position. However, since the needle holder axis 6 a can be moved, the needle holder axis 6 a can be positioned at any angle between the first position (substantially perpendicular to the first guide 1) and the maximum inclined position at a maximum inclination angle θ3=θ1+θ2. The position of the needle holder 6 can be achieved by the displacement of the needle holder axis 6 a around the axis 3 a and/or the axis 1 a of the rotary guides 3 and 1, respectively.

More specifically, as the second rotary guide 3 rotates around its rotational axis 3 a, the needle holder axis 6 a is displaced (travels) around a cone formed by the inner diameter of second rotary guide 3 and the crossing point 9. This cone will be referred to as a first cone of acceptance. FIG. 3B illustrates a position where the needle holder axis 6 a has been displaced to a predetermined position around the circumference of the second rotary guide 3 from that shown in FIG. 2B. That is, as shown in FIG. 3B, the needle holder axis 6 a has been displaced around the first cone of acceptance.

Similarly, as the first rotary guide 1 rotates around its rotational axis 1 a, the axis 3 a of the second rotary guide 3 is displaced (precesses) around the axis 1 a. Since the axis 1 a and axis 3 a are fixed at the crossing point 9, the precession of axis 3 a around the axis 1 a defines another cone, which will be referred to herein as a “second cone of acceptance”. The second cone of acceptance is formed by the circumference defined by axis 3 a and the crossing point 9 with respect to the axis 1 a, as the first rotary guide 1 rotates around its axis 1 a.

It should be recognized therefore, that needle placement can be effected at the fixed crossing point 9 from anywhere within the first cone of acceptance and/or the second cone of acceptance. FIGS. 3A, 3B and 3C illustrate in explicit detail some examples of needle insertion at crossing point 9 with various angles of insertion. In FIG. 3A, the first cone of acceptance is formed when the second rotary guide 3 rotates around its own axis of rotation 3 a. In FIG. 4A, it is assumed that the first rotary guide 1 is fixed (does not rotate). In this assumed fixed position of the rotary guide 1, the needle holder 6 can be displaced (rotated) to point around the base on the first cone of acceptance, but one point of the needle holder axis 6 a will be fixed at crossing point 9. Now it is assumed that the second rotary guide 3 stops rotating.

Turning now to FIG. 3B, the second cone of acceptance is formed when the first rotary guide 1 rotates around its own axis of rotation 1 a. In FIG. 3B, it is assumed that that second rotary guide 3 is fixed (does not rotate). In the assumed fixed position of the second rotary guide 3, since the first rotary guide 1 is connected to the second rotary guide 3 via the rotation body 2 (pillars 2 a-2 c), the needle holder 6 can be displaced (rotated) to any point around the base of the second cone of acceptance, but the one point of the needle holder axis 6 a will still remain fixed at crossing point 9. In this manner, the needle holder 6 can be positioned at any angle between the perpendicular position and the maximum inclined position.

FIG. 3C illustrates that both the first and second cones of acceptance can be used to position the needle holder 6 at a desired position and angle, while still maintaining one point of the needle holder axis 6 a at the crossing point 9. More specifically, FIG. 3C illustrates that both the first rotary guide 1 and the second rotary guide 3 can be rotated simultaneously (or separately) around their corresponding axis 1 a and 3 a. In this manner, the second rotary guide 3 can rotate around its axis 3 a and can precess around the axis 1 a of the first rotary guide 1.

Therefore, arranging the crossing point 9 at the desired needle insertion point of the skin 8, allows a clinician to insert the needle 7 from any angle within an acceptance cones allowed by rotation of the rotary guides 1 and 3. In this manner, the target tissue 8 a can be reached from different incision angles without changing the position of the inserting point. In addition, since the needle may be inserted from any angle within a cone of acceptance, with this manipulator a clinician can treat different regions of the tissue through only one insertion point on the patient's skin.

Referring now to FIGS. 4A and 4B a description is provided for a maximum angle of inclination 63 and optimal use of rotational space determined by the maximum angle of inclination 63. As illustrated in FIG. 4A, the actual usable space within the cones of acceptance for the needle holder 6 can be limited by the arrangement of the second rotary guide 3 in a slanted orientation with respect to the first rotary guide 1, above the base body 5. In FIG. 4A, T indicates the approximate height from a contact surface, e.g., a patient's skin 8 to an upper surface of the first rotary guide 1 above the base of base body 5 (i.e., above the needle incision point or crossing point 9); and R indicates the internal radius of the free space within the first rotary guide 1. Preferably, the point of needle incision or crossing point 9 is located at the geometric center at the bottom of the first rotary guide 1. In addition to the height of the first rotary guide 1, the needle holder 6 attached to the second rotary guide 3 occupies certain space above the base body 5, and the needle holder 6 requires a minimum of inclination with respect to the crossing point 9. When all of these parameters are taken into consideration, it is estimated that the needle holder axis 3 a can have an maximum inclination θ3 defined by equation (1), as follows:

θ1+θ2≦θ3=π/2−tan⁻¹(T/R)  (1)

Equation (1) provides the condition when all 360 degrees (a complete rotation) can be used for the second (tilted) rotary guide 3. However, to reach to the limit of equality of equation (1), the tilted second rotary guide 3 may need to be larger than the first rotary guide 1 and/or the tilted second rotary guide 3 may need to be positioned outside of the horizontal first rotary guide 1. Accordingly, a person of ordinary skill in the art will understand the embodiments disclosed herein can be modified to have the second rotary guide 3 outside the first rotary guide 1 and yet maintain a maximum inclination angle θ3 provided by equation (1).

Referring to FIG. 4B, it can be appreciated that the needle 7 extending along the needle holder axis 6 a will encounter a physical obstacle in the horizontal first rotary guide 1. This limits the rotation of the second rotary guide 2 to a space [1] within a maximum allowable space [2]. Specifically, due to above-discussed actual size and arrangement of the rotary guides 1 and 2, as observed from a view direction A (shown in FIG. 4A), the maximum allowable usable space for maneuvering the needle holder 6 is an space [2] shown in FIG. 4B. However, the tilted second rotary guide 3 needs not use the entirety of space [2]. Indeed, only half of space [2] can be used because whatever orientation of the needle holder 6 in that half-range of space [2] can also be oriented within the other half-range by using the rotation of the horizontal first rotary guide 1. That is, rotating both the first rotation guide 1 and the second rotation guide 3 allows the positioning of the needle holder 6 any part of the maximum allowable space [2]; this was already illustrated in a more generalized manner in FIG. 3C.

Second Embodiment

FIGS. 5A and 5B are sectional views of a needle placement manipulator 200, in accordance with a second embodiment. FIG. 6 is a detailed sectional view of the left side of FIG. 5A. The second embodiment is substantially similar to the first embodiment. One notable difference in the needle placement manipulator 200, according to the second embodiment, is that the manipulator 200 includes motorized actuators for the rotation of first and second rotary guides 1 and 3.

Specifically, in this embodiment, the first rotary guide 1 now includes a rotation drive unit 210, and the second rotary guide 2 includes a rotation drive unit 220. In the first rotary guide 1, the rotation drive unit 210 comprises a piezoelectric actuator 11, a rotary slider 12, a ball-bearing 13, a screw part 14, a pressurized means 15, a first electric cable 16, a position sensor 17, a rotary scale 18, a second electric cable 19, and an external casing 1.1 and internal casing 1.2.

As shown in FIG. 6A, the piezoelectric actuator 11 comprises a vibrator body 11 a and piezoelectric material 11 b. The piezoelectric material 11 b is fixed to vibrator body 11 a with adhesive. The piezoelectric material 11 b embeds a plurality of electrodes (not drawn) which apply electric voltage to the piezoelectric material 11 b. Piezoelectric actuator 11 is supported through pressurized means 15 to internal casing 1.2 of the rotary guide 1. External casing 1.1 and internal casing 1.2 are relatively rotatable by bearing 13 which is fixed by the screw part 14. The rotary slider 12 is fixed to external casing 1.1. The piezoelectric actuator 11 and rotary slider 12 are pressurized against each other by pressurized means 15. Applying a driving voltage to electrodes of piezoelectric material 11 b through electric cable 16, the vibrator body 11 a vibrates and the rotary slider 12 is driven by frictional force between actuator 11 and rotary slider 12. Internal casing 1.2 is driven by the piezoelectric actuator. In the present embodiment, the pressurized means 15 can be implemented by a coil spring, but it can also be a pressure plate, a wave washer spring, or like pressing devices. The piezoelectric actuator 11 may, in some applications, be exchanged for an electrostrictive actuator.

The position sensor 17 is attached to the surface of internal casing 1.2. Rotary scale 18 is mechanically attached to the surface of the rotary slider 12. Electric power supply to position sensor 17 and detected signals thereof are transferred by electric cable 19. Position sensor 17 detects relative rotational position by detecting the rotary scale 18.

In the second rotary guide 2, the rotation drive unit 220 is substantially similar to rotation drive unit 210. Rotation drive unit 220 comprises a piezoelectric actuator 21, a rotary slider 22, a bearing 23, a screw part 24, a pressurized means 25, a first electric cable 26, a position sensor 27, a rotary scale 28, a second electric cable 29, an external casing 2.1 and internal casing 2.2.

Structure of second rotary guide 2 is similar to first rotary guide 1. A structural difference of second rotary guide 2 from first rotary guide 1 is that the function of external casing 2.1 and internal casing 2.2 are interchanged. The piezoelectric actuator 21 is supported through the pressurized means 25 to external casing 2.1. Position sensor 27 is also fixed to external casing 2.1. Rotary slider 22 is fixed to internal casing 2.2.

In the embodiment shown in FIG. 6A, only one position sensor and one actuator for each of the guides 1 and 3 have been shown for the sake of clarity in the illustration. The position sensors and actuators may be installed more than one to each of the guides. In this manner, additional position sensors and actuators can be provided to be used as backup or supplemental to the first ones in various instances of the operation of the manipulator to increase reliability, stability and precision of the manipulator.

As in the first embodiment, the manipulator 200 of the second embodiment is constrained to operate needle positioning within a maximum available space [2] determined by the tilted arrangement of the second rotary guide 3 with respect to the first rotary guide 1, as discussed in reference to FIGS. 4A and 4B. With such arrangement, as illustrated in FIG. 5B, the needle manipulator 200 is configured to position the needle at any position between a substantially perpendicular position (where θ=0 degrees) and a maximum angle of inclination θ3 determined by equation (1).

<Available Exemplary Materials for Rotation Units 210 or 220>

Certain Available Exemplary Materials for rotation drive units 210 or 220 may be selected, as follows:

Vibrator body: non-magnetic metal, ceramics (e.g., alumina, zirconia, partially stabilized zirconia), and other non-magnetic materials;

Rotary slider: engineering plastic material such as polytetrafluoroethylene (PTFE), polyether ether ketone (PEEK), polyimide (PI), Polyamide-imide (PAI), Polyphenylene sulfide (PPS), fiber reinforced plastic material such as carbon filled, glass fiber filled, or ceramics material;

Bearing: ceramics, plastic, air bearing;

Position sensor: optical-electrical type, fully optical (optical fiber);

Scale: print on plastic sheet, molded plastic, glass grating, etc.;

Position sensor and index scale may be implemented in various different manners. For example, it can be implemented by micro optical encoders. Alternatively, it can be implemented as a purely optical sensor, by using optical fibers.

FIG. 6B illustrates a variation of the second embodiment where, in the first rotation drive unit 210, a light source fiber fs1 delivers light to the rotary scale 18 and a collecting fiber fd1 is used to detect light reflected from the rotary scale 18. Similarly, in the second rotation drive unit 220, a light source fiber fs2 delivers light to the rotary scale 28 and a collecting fiber fd2 is used to detect light reflected from the rotary scale 28. The use of optical fibers may be particularly desirable to avoid the use of electrical wiring for minimizing noise and interference in the MRI system, in particular to avoid interference with RF-pulse signals.

Advantageously, in the second embodiment, accurate positioning up to an order of microns can be implemented by the use of optical rotary position sensors and piezoelectric actuators. Accurate positioning is available by piezoelectric actuator and feedback signaling, which can be automated by controllers operated with programmed algorithms. At least two piezoelectric vibrators and two position sensors are arranged into the parts which are not relatively movable. Arranging the piezoelectric vibrators and position sensors within non-movable parts permits that all electric cables can be tied into one bundle. Therefore, shielding of electric cables to decrease noises which MRI receives can be simplified. The manipulator can be moved without entangling of cables, so arrangement of electric cables can be simplified.

Conventionally, prior to every needle incision operation, the needle holder 6 and the base body 5 must be sterilized because they are touched by clinician and patient. In accordance with embodiments disclosed herein, base body 5 and other parts fixed to external casing 1.1 can be made of disposable and recyclable materials, such as plastic. In this manner, these parts can be disposable in one clinical procedure. The needle holder 6 and the internal casing 2.2 can also be made of disposable materials. In this manner, the characteristics of piezoelectric actuators are stable because the friction surface of the rotary slider which faces to piezoelectric vibrator is a new surface in each clinical procedure.

Arranging piezoelectric actuators and rotary sliders to be ring or arc shape to be fit to the circular shape of rotary guides, the manipulator can be motorized to be automated, and yet maintain a small size. Holding torque of piezoelectric actuator stabilizes the manipulator in a stop state. Alternatively, stop screws as those provided in the first embodiment may be arranged within the external casing 1.1 so that a clinician may optionally secure the rotating guides with the screws, in addition to the piezoelectric actuator stop. FIG. 7A illustrates an example of a motorized manipulator 200, in accordance with a modification of the second embodiment. In FIG. 7A, set screws 201 and 203 are used as a locking mechanism for locking the rotational guides 1 and 3, respectively, in a stopped position. Stop set screws can be advantageous in a case where there is possibility of unexpected rotating force being applied to the rotary guides, while the piezoelectric actuator keep its stopped position only by friction, for example.

FIG. 7B illustrates a further modification to the needle manipulator 200 in accordance with the second embodiment. In FIG. 7B, the base body 5 includes a fitting and sliding portion 5 a in which the first rotary guide 1 is disposed (fitted) with a certain degree of tolerance, such that the first rotary guide 1 slides in a vertical direction V perpendicular to the bottom surface of base body 5. When the first rotary guide 1 is allowed to slide in the vertical direction V (perpendicularly) with respect to the bottom surface of base body 5, a distance h (height) between the bottom surface of the base body 5 and the first rotary guide 1 can be selectively adjusted. Once the rotary guide 1 is located at a desired distance or height h with respect to the bottom surface of base body 5, the first rotary guide 1 is locked in place by a height locking mechanism, such as a set screw 51. In this manner, it is possible to adjust the position (height or distance) of the crossing point 9 with respect to a target surface (e.g., the skin 8 of a patient's body). In this embodiment, even when the position (height) of crossing point 9 is changed along the axis 1 a of the first rotary guide 1, the rotational axis 1 a of the first rotary guide 1, the rotational axis 3 a of the second rotary guide 3, and the needle holder axis 6 a still cross each other at a single crossing point 9. Advantageously, the crossing point 9 can be adjusted to the target surface to, for example, accommodate the various shapes of a patient's body parts. In this embodiment, it should be noted, that when the rotary guide 3 is made to slide vertically with respect to the base body 5, the set screw 201 will also slide in the V direction together with the rotary guide 1. To that end, the sliding portion 5 a of base body 5 should be modified to include a hollow portion 5 b to allow vertical displacement of the set screw 201.

Third Embodiment

A third embodiment is now described with respect to FIGS. 8A, 8B and 9. A needle manipulator 300, in accordance with the third embodiment is substantially similar to the manipulator 100 of the first embodiment in that needle positioning is effected by manually rotating the rotary guides 1 and 3. A notable difference in the third embodiment, in contrast to the first one, is that the manipulator 300 includes an attached RF-coil.

Specifically, FIG. 8A is a perspective view of manipulator 300 and FIG. 8B is a perspective view of the manipulator 300 showing a vertical cut along plane H-H, in accordance with third embodiment. FIG. 9A is a sectional view of the manipulator 300 cut along the vertical plane H-H, according to the third embodiment. The needle manipulator 300 of the present embodiment may be particularly suitable for use in MRI-guided percutaneous interventions. In this embodiment, the manipulator 300 includes attachments for an RF-coil which is used in a MRI-scanner. The structure for positioning needle 7 is basically the same as the one described in first embodiment.

As illustrated in FIG. 8A, the manipulator 300 includes a first attachment 30 and a second attachment 31 to fix the manipulator 300 to a single loop RF-coil 32. The first attachment 30 is placed directly on a patient such that a bottom surface of the first attachment 30 rests on the patient's skin, for example. The needle manipulator 300 includes a plurality of fiducial markers 10 a, 10 b, 10 c and 10 d in the first rotary guide 1 and fiducial markers 10 e, 10 f, 10 g through 10 h (10 e not shown) on the second rotary guide 3, as described in the first embodiment. In addition, at least the first attachment 30 includes fiducial markers 33 a, 33 b, 33 c and 33 d (markers 33 c and 33 d are not seen in FIG. 8A). Since the first attachment 30 remains fixed to the body of the subject under examination, the fiducial markers 33 a-33 d serve as a reference, so that needle position and orientation can be tracked with fiducial markers located on either one or both of the guides (e.g., fiducial markers 10 a-10 h).

FIG. 8B illustrates a perspective view of the manipulator 300 mounted onto RF-coil 32 in which a sectional cut along vertical plane H-H is performed. FIG. 9A illustrates a sectional view of the needle placement manipulator cut along a vertical plane H-H, according to the third embodiment. The first attachment 30 includes a flat setting portion on which the RF-coil 32 is set, and a circular projection portion 30 a configured to engage with the second attachment 31. Similarly, the second attachment 31 includes a flat setting portion below which the RF-coil is set, and a circular projection portion 31 a which engages with the projection portion 30 a of the first attachment 30.

As illustrated in FIG. 9A, the single loop RF-coil 32 is placed with the circular projection 30 a of attachment 30 going through the opening of the RF-coil 32. The second attachment 31 is fixed to the base body 5 and the circular projection section 31 a is disposed at the bottom surface thereof. These two attachments 30 and 31 are configured to be engaged (fitted) by the two circular projections 30 a and 31 a, respectively, such that the two attachments remain fixed at relative positions while securing the RF-coil 32 therebetween. Fixing the two attachments 30 and 31 at relative positions can be done by one or more set screws (not shown), or by force fitting (pressure), or by one or more air chucks (not shown), or by any other mechanical means that will prevent unexpected movement or dislodging between the two attachments.

FIG. 9B illustrates a detailed view of section A shown in FIG. 9A where a first attachment 30 engages with a second attachment 31 on an outer surface thereof. FIG. 9C illustrates a detailed view of section A shown in FIG. 9A where a first attachment 30 engages with a second attachment 31 on an inner surface thereof. Regardless of how the two attachments have been joined, the two attachments 30 and 31 are engaged (fitted) into each other by the two circular projections 30 a and 31 a, respectively, such that the two attachments remain fixed at relative positions while securing the RF-coil 32 therebetween. Notably, as shown in FIGS. 9B and 9C, the second attachment 31 may be integrated into the base body 5. In this manner, the base body 5 and the second attachment 31 are integrally attached as a single mechanical structure. Moreover, the second attachment 31, the based body 5 and the non-movable portion of the first guide 1 can be integrally formed as a single mechanical structure. Making the second attachment 31 an integral part of base body 5, or making the second attachment 31 with base body 5 and part of the first guide 1 an integral structure may facilitate prompt attachment and detachment of the needle manipulator 300 onto the RF-coil 32. However, as described above, the attachment 31 may be removably attached to the base body 5.

Once the two attachments are assembled with the manipulator 300, the axis 1 a of the first rotary guide 1, the axis 3 a of the second rotary guide 3 and the needle holder axis 6 a of the needle holder 6 are arranged to cross at a single crossing point 9. The crossing point 9 is preferably located at the center of gravity of manipulator 300, which should be located at the geometric center of the bottom surface of first attachment 30. Fitting part of circular projections 31 a and 30 a can be replaced by screw adjustment, so that the crossing point 9 is adjustable with respect to the patient's skin, as shown in FIG. 7B.

If the RF-Coil includes a plurality of openings, like a body matrix coil, the RF-coil attachment 30 is prepared according to the shape of each opening. If the opening of the RF-coil is of a square shape, attachment 30 should be made in a square shape too, and attachment 31 should be made to adapt, on one side, to the shape of the base body 5, and on the other side to the attachment 30.

Turning now to FIGS. 10A through 10C, a description is provided of an exemplary procedure for attaching and detaching the manipulator 300 and RF-coil 32 onto a body of a target patient. FIG. 10A shows a first attachment 1001 with an upward protruding ring (protrusion section), a single loop RF-coil 1002, and a second attachment 1003 with a downward protruding ring. In FIG. 10A, the first attachment 1001 with its protruding ring facing upward is first set on a patient (the subject of needle placement), and the second attachment 1003 with the protruding ring facing downward is attached to base body 5 of the needle manipulator. The protruding ring of first attachment 1001 is arranged to engage with the protruding ring of the second attachment 1003. In FIG. 10B, the RF-coil 1002 is set on the first attachment 1001. The opening of RF-coil 1002 is loosely fit around the protruding ring of the first attachment 1001, so that the RF-coil 1002 can be rotated or moved to adjust the positioning of cabling and other parts (not shown in the figure). In FIG. 10C, the needle manipulator unit is set onto the first attachment 1001. The second attachment 1003, which is the part protruding downward from the needle manipulator unit, engages firmly with the first attachment 1001 so that needle position and orientation with respect to the patient can be accurately known, by tracking the fiducial markers. FIG. 11 is a perspective view of the assembled needle manipulator attached to the RF-coil 1002 and the first and second attachments 1001 and 1003.

Certain Advantages in the third embodiment are that the opening of RF-coil and the manipulator's opening (space through which the needle is inserted) are made to coincide with each other. In this manner, the opening can be advantageously utilized for a clinician's access to entry point (incision point) of a patient's skin. The RF-coil 32 and manipulator 300 are removably combined into one unit, so that clinical procedure could be simple.

Fourth Embodiment

A fourth embodiment is now described with respect to FIG. 12. A needle manipulator 400, in accordance with the fourth embodiment is substantially similar to the manipulator 200 described above in reference to the second embodiment. A notable difference in the fourth embodiment is that the needle manipulator 400 includes motorized rotational guides 1 and 3, and an attached to RF-coil 32.

Needle positioning in the manipulator 400 of the forth embodiment is automated with piezoelectric actuators and optical sensors. In the present embodiment, a second attachment 31 and the base body 5 can be combined into a single body.

In this manner, RF-Coil's opening and manipulator's opening are made to coincide with each other and utilized for clinician's access to entry point of patient's skin. The positioning accuracy of the manipulator with respect to the subject of the needle placement is improved by directly positioning the first attachment to the patient and the capability of attaching the manipulator to the first attachment with high repeatability. The piezoelectric actuator can guarantee precise positioning and steady fixation (stop); this prevents movement of the manipulator 400 even when movement of the patient occurs. In addition, in an automated robotic application, the actuators can be controlled by a controller (CPU) with programmed algorithms designed so that automatic position adjustment occurs in response to patient movement.

Fifth Embodiment

FIG. 13 illustrates block diagram of an automated image-guided needle positioning system 500 which includes a motorized manipulator, and can be programmed for automatic (e.g., remote or robotic) manipulation, in accordance with a fifth embodiment. FIG. 13 is a block diagram of the image-guided needle positioning system 500. In accordance with present embodiment, the block diagram shows a function performed by each block included in the system 500. Each function may be implemented purely in hardware and/or a combination of software and hardware.

An image guided needle positioning system 500 includes namely the following main functional blocks: a needle placement manipulator 510, an MRI-system 520, image guide system 530, a manipulator controller 540, and an actuator controller 550. All of the functional blocks are interconnected by circuit or network connectivity. Some of the blocks may be integrated into a single block provided that he combined block still performs the functionally of each block. The needle placement manipulator 510 corresponds to any of the first or second embodiments disclosed herein, as long as an actuator 512 and a sensor 514 can be implemented within the manipulator. The needle placement manipulator 510 including the RF coil 516 corresponds to any of the third and fourth embodiments disclosed herein.

The MRI guide system 530 includes an image monitor (image display) 531, an input device module 532 (e.g., keyboard, mouse, touchpad, etc.), a central processing unit (CPU) implemented by one or more microprocessors, hardware memory 534 (volatile and non-volatile memory and storage devices, such a hard drives may be included), and an Image Guide Software module 535. The image guide software module 535 includes, among other things, programmed algorithms to communicate and control each of the other functional blocks. An example of such image guided application is described by Song et al., in a non-patent literature article entitled “Biopsy Needle Artifact Localization in MRI-guided Robotic Transrectal Prostate Intervention,” IEEE transactions on Biomedical Engineering, July 2012.

Image guide system 530 acquires images of a target patient or body-part thereof, of the fiducial markers of in manipulator and RF-coil base (see, e.g., FIG. 8A), and of the needle 7. The manipulator controller 540 communicates with actuator controller 550 for needle positioning. Actuator controller 550 drives piezoelectric actuator 512 or USM (ultrasonic) motor and controls the driving with position sensor 514 in closed-loop control. Kinematics calculator 542 translates the signals from the image guide system 530 into control signals for the actuator controller 550. Actuator controller 550 is implemented in hardware for controlling an actuator (e.g., piezoelectric actuator or USM motor). Position controller 552 may be implemented in software and/or hardware. The position controller 552 calculates a control amount for the actuator 512 so that the needle moves in a target orientation angle based on signal output from a position sensor 514.

In the case of operating under the magnetic field of an MR-based modality (MRI system 520), the static magnetic field magnet 522 generates a static magnetic field in the imaging space. The gradient coil 524 generates a gradient magnetic field in the X-axis direction, a gradient magnetic field in the Y-axis direction and a gradient magnetic field in the Z-axis direction in the imaging space.

An RF transmitter 526 outputs RF pulses (RF current pulses) to the RF coil 516. The RF coil 516 transmits the RF pulses to the human body. The RF coil receives an MR signal generated due to excited nuclear spin inside the human body according to the RF pulse. An RF receiver 528 detects the MR signal. Then, the detected data or a signal based on the detected data is input into an image guide system 530. Volumetric MRI scans can confirm the position and orientation of the needle's tip, based on fixed reference fiducials (e.g., disposed on the RF-coil attachments) and movable fiducials disposed on at least one of the rotary guides. Forward Kinematic Mapping (FKM) can be implemented in the position controller 552 to iteratively drive the needle to a desired target position and to even compensate for positional errors. It is envisioned, for example, an arrangement where, for every needle incision, the position of the manipulator and patient can be registered with respect to the coordinates of the MRI system. During a needle incision procedure, the position of the tip of the needle is also registered with respect to the manipulator, the patient and the MRI system. Then a forward kinematic algorithm performs calculations for controlling the manipulator and updating the position and orientation of the tip of the needle. To ensure precision of needle placement, a safety routine that continuously compensates for needle artifacts can be added to the algorithm.

Other Embodiments and Modifications

In the embodiments disclosed above, various combinations and modifications will be readily evident to persons having ordinary skill in the art. As discussed above with respect to FIGS. 4A and 4B, for example, the needle manipulator may be modified to include a second rotary guide 3 having a diameter larger than a diameter of the first rotary guide 1. This modification can allow for the second rotary guide 3 to be placed outside of the first rotary guide 1 instead of inside, as shown in all of the first to fourth embodiments. In addition, although the third to fifth embodiments are directed to MRI-based image guided needle manipulators, the needle manipulators disclosed herein may be applicable to other imaging modalities, such as ultrasound, mammography, computed tomography (CT) and the like. When applied to other modalities, the fiducial markers need not be readable by MRI-scanners as disclosed above. Instead, the fiduciary markers can be modified to conform to the specific imaging modality, or can be removed.

In each of the first to fourth embodiments, the first rotary guide 1 is supported by the base body 5 and connects to a first rotation body 2. The second rotary guide 3 is supported by the first rotation body 2 at a slated angle with respect to the first rotary guide 1. The first rotation body 2 may be of a fixed height it can change in height, such that the second rotary guide 3 can be positioned from substantially parallel to substantially perpendicular to the first rotary guide 1. In this manner, positioning of a needle by the needle holder 6 can apply to other than the maximum angle of rotation and optimal rotation space discussed above.

While the present invention has been described with reference to exemplary embodiments, it is to be understood that the invention is not limited to the disclosed exemplary embodiments. The scope of the following claims is to be accorded the broadest interpretation so as to encompass all such modifications and equivalent structures and functions. 

What is claimed is:
 1. A needle placement manipulator comprising: a needle holder which holds a needle along an insertion axis; a guide to position the axis of needle holder to a predetermined direction; a base body on which the guide is supported; a first attachment including a base surface and a setting portion on which RF-coil is set; a second attachment connected to the base body and including an attaching portion which attaches the second attachment to the first attachment, wherein the base surface of the first attachment is configured to be the closest plane of the manipulator to a subject of the needle placement.
 2. The needle placement manipulator according to claim 1, wherein the guide includes first rotary guide which is fixed to the base body and second rotary guide which is fixed to the needle holder with their axes of rotation at a first angle with respect to each other.
 3. The needle placement manipulator according to claim 1, wherein the first attachment and the second attachment have opening region around the axis of needle.
 4. The needle placement manipulator according to claim 1 wherein the guide is a rotary guide which has opening around the axis of needle.
 5. The needle placement manipulator according to claim 1, wherein the guide includes first rotary guide and second rotary guide with their rotational axis are fixed at a first angle with respect to each other.
 6. The needle placement manipulator according to claim 5, wherein the second rotary guide and the axis of the needle holder are fixed at a second angle with respect to each other, and wherein the second angle is greater than or equal to the first angle.
 7. The needle placement manipulator according to claim 5, wherein two rotational axes of the two rotary guides and the axis of needle holder are crossed at one point.
 8. The needle placement manipulator according to claim 7, wherein the crossing point is on the plane of the base surface of the first attachment.
 9. The needle placement manipulator according to claim 1 wherein at least one actuator is arranged in the guide.
 10. The needle placement manipulator according to claim 1, wherein at least one position sensor is arranged in the guide.
 11. The needle placement manipulator according to claim 9, wherein the actuator includes piezoelectric material.
 12. The needle placement manipulator according to claim 11, wherein the actuator includes slider part which is pressurized to friction element fixed to piezoelectric material by pressurized means and relatively actuated by the vibration of a vibrator.
 13. The needle placement manipulator according to claim 11, wherein the actuator includes vibrator body to which piezoelectric material is fixed and a slider part which is pressurized to vibrator body by pressurize mean and relatively actuated by the vibration of the vibrator.
 14. The needle placement manipulator according to claim 13, wherein the vibrator body is made by ceramic material.
 15. The needle placement manipulator according to claim 12, wherein the slider part includes resin material.
 16. The needle placement manipulator according to claim 12, wherein the friction element includes resin material
 17. An image guided needle positioning system comprising: a needle placement manipulator according to claim 1; an RF-coil; an MRI-system which acquires an image of a target area of a subject, an image of needle placement manipulator and an image of the needle; an image guide system which indicates a needle orientation angle for targeting the target area of the subject; a manipulator controller which receives the needle orientation angle and calculates two positions of the guide based on the images acquired by the MRI-system; a motor controller which communicates to a manipulator controller, drive and control motor supplying driving power to motor and position sensor and receiving position signal from position sensor.
 18. A needle placement manipulator according to claim 1, wherein the setting portion of the first attachment includes a projection portion which goes through an opening of the RF-coil, and the second attachment is attached rigidly to the projection portion.
 19. A needle placement manipulator comprising: a needle holder configured to hold a needle; a guide system configured to position the needle holder to a predetermined direction with respect to a subject of needle placement; an attachment including an attaching portion to which the guide system is attached and a setting portion on which an RF-coil is set, and wherein a base surface of the setting portion is configured to be disposed on the subject.
 20. The needle placement manipulator according to claim 19, wherein the guide system is rotary guide system, and an axis of the needle holder and an axis of the rotary guide system cross at a crossing point located on a plane parallel to the base surface.
 21. The needle placement manipulator according to claim 20, wherein the rotary guide system includes a first rotary guide and a second rotary guide.
 22. The needle placement manipulator according to claim 21, wherein the second rotary guide is disposed at an slated angle with respect to the first rotary guide.
 23. The needle placement manipulator according to claim 22, wherein an axis of the first rotary guide, an axis of the second rotary guide and the axis of the needle holder cross at the crossing point.
 24. The needle placement manipulator according to claim 20, further comprising a distance adjustment mechanism configured to adjust the plane on which the crossing point is located.
 25. The needle placement manipulator according to claim 24, wherein the distance adjustment mechanism varies a distance from the base surface of the setting portion to the crossing point such that the crossing point is located at the plane parallel to the base surface above the base surface or below the base surface. 